Disease: C-reactive protein measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs651007 0.851 0.160 9 133278431 upstream gene variant T/A;C snv 22
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs2126259
LOC157273
1.000 8 9327636 intron variant T/C snv 0.87 9